Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP522469.RAFno-hOcY_xgSaPI8W9-x3lijlYlGgGxPFl28zy48fEQ130_assertion> ?p ?o ?g. }
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- NP522469.RAFno-hOcY_xgSaPI8W9-x3lijlYlGgGxPFl28zy48fEQ130_assertion type Assertion NP522469.RAFno-hOcY_xgSaPI8W9-x3lijlYlGgGxPFl28zy48fEQ130_head.
- NP522469.RAFno-hOcY_xgSaPI8W9-x3lijlYlGgGxPFl28zy48fEQ130_assertion wasGeneratedBy ECO_0000203 NP522469.RAFno-hOcY_xgSaPI8W9-x3lijlYlGgGxPFl28zy48fEQ130_provenance.
- NP522469.RAFno-hOcY_xgSaPI8W9-x3lijlYlGgGxPFl28zy48fEQ130_assertion wasDerivedFrom befree-20150227 NP522469.RAFno-hOcY_xgSaPI8W9-x3lijlYlGgGxPFl28zy48fEQ130_provenance.
- NP522469.RAFno-hOcY_xgSaPI8W9-x3lijlYlGgGxPFl28zy48fEQ130_assertion SIO_000772 20560207 NP522469.RAFno-hOcY_xgSaPI8W9-x3lijlYlGgGxPFl28zy48fEQ130_provenance.
- NP522469.RAFno-hOcY_xgSaPI8W9-x3lijlYlGgGxPFl28zy48fEQ130_assertion evidence source_evidence_literature NP522469.RAFno-hOcY_xgSaPI8W9-x3lijlYlGgGxPFl28zy48fEQ130_provenance.
- NP522469.RAFno-hOcY_xgSaPI8W9-x3lijlYlGgGxPFl28zy48fEQ130_assertion description "[Identification of a Kir3.4 mutation in congenital long QT syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522469.RAFno-hOcY_xgSaPI8W9-x3lijlYlGgGxPFl28zy48fEQ130_provenance.